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Introduction
Chapter
1
Chapter
2
Chapter
3
Chapter
4
Chapter
6
Chapter
7
Epilogue |
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In the not-too-distant past,
most people assumed that mankind could be divided into subcategories of
people whose skin color, body shape or facial features were different
enough to mark them as members of distinct races within the human species.
Many people still make this assumption. To them, the claims of the Lemba
people, a remote tribe living in the northeast corner of the Union of
South Africa, are problematic. The Lemba insist that their practice of
circumcision, their avoidance of eating pork and an oral history that
traces their origins to the Middle East prove that they are Jews-and Jews
by descent, not by conversion.
The
Lemba are black. They believe that their ancestors came from the land
of Israel, probably passed through southern Arabia and, centuries ago,
crossed over into Africa. But they certainly don't look "Jewish," and
the mainstream Jewish community has not taken their claim of kinship to
heart. If they really are Jews, what does this tell us about our assumptions
of racial identity?
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Dui Seid
Bloodlines, 1998
photographic projection, encaustic, wood, glass and plastic
"I feel that my interest in science
always related to and affected my art, because art, in many ways, is
seeking a personal truth. And I felt that science was also seeking a
truth, an absolute physical truth-or, let's say, laws.
I felt that there was an affinity between the two-they were not the
antithesis to each other that often people in the arts assume."
- Dui Seid
To
see an interview with Dui Seid, click here
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As recently
as 1962, Carleton Coon, a prominent anthropologist, published a best-selling
book called The Origin of Races, which neatly divided human beings into
five "races" he called Caucasoid, Mongoloid, Australoid, Negroid, and
a group he called Capoid (named for the Cape of Good Hope). In this last
category, Coon lumped together southern tribes, like the Bushmen and Hottentots,
and some tribes from eastern Africa who had dark skin but did not otherwise
fit well into his description of Negroid people. He speculated that since
there were pygmies among them, perhaps they had a genetic propensity to
shrink. Coon argued that these races were descendants of five different
subspecies of humans that had existed in the Middle Pleistocene era and
had evolved independently into races of Homo sapiens. According to Coon,
the Caucasoids, who he believed had evolved first, were by implication
a bit further up the ladder of civilization.
Coon,
like most physical anthropologists, based his distinctions among races
on observable characteristics such as skin and eye color, facial features
and body shape-what contemporary biologists call the phenotype. Today,
human geneticists have begun to group people according to less visible
markers-the genes we carry on the chromosomes in each of our cells. Biologists
call this the genotype.
Just
as paleontologists now rely on carbon dating to ascertain the age of fossils
and inorganic objects like the stones in Stonehenge, molecular biologists
now look to the genotype to trace human heredity. Within each of their
body's cells, human females carry mitochondria, tiny entities that have
their own DNA. Mitochondrial DNA enables geneticists to track characteristics
that are passed from mother to daughter. In contrast, all human males
carry a Y chromosome, which is passed from father to son and remains remarkably
stable down through generations.
Late
in 1997, a group of British geneticists embarked upon a curious enterprise.
They gathered DNA samples from a randomly chosen group of Jewish men enjoying
themselves at a beach in Tel Aviv. Some of the men, because their surnames
were variations of the name Cohen, could claim to be members of the priestly
tribe of Cohanim, which by tradition traced its ancestry back to the biblical
tribe of Levi. Since membership in this priesthood is transferred from
father to son, researchers decided to look for distinctive patterns on
the men's Y chromosomes.
A particular
set of genetic markers that are extremely rare in the non-Jewish population
showed up in about 10 percent of the Tel Aviv beachboys. This marker is
suggestive of Jewish ancestry whenever it is found; it probably existed
in the ancestral Hebrew population and was passed on through the centuries
to males in contemporary Jewish communities. But most astounding was the
discovery that these markers appear in over 50 percent of men who claim
to be Cohanim. Thus, the markers came to be called the Cohen Modal Haplotype.
The
English geneticists were on a roll. They then collected DNA samples from
men of the Lemba tribe, as well as from the males in a group of Yemenites
still living in the region of southern Arabia from which the Lemba traditions
indicated they had lived before they migrated to southern Africa. They
found sufficient genetic similarities between the Lemba and the current
Yemenites to suggest that they are kinsmen.
But
are they Jews?
The
geneticists found that the proportion of Lemba men carrying the genetic
signature of Cohanim was about 10 percent, similar to the percentage found
among Jewish men around the world and much higher than found in the general
population. Moreover, the Cohen Modal Haplotype appeared in about half
of one particular group of Lemba-the Buba clan, the most prestigious of
all Lemba clans. This is strong evidence that the Lemba are genetically
connected to worldwide Jewry and that the Buba clan are not only Jewish,
but belong to the hereditary priestly class.
This
genetic bulletin provides validation for the Lemba and important news
to the worldwide Jewish community about their far-flung cousins. But it
is equally fascinating for what it tells everyone about race. This surprising
genetic link between a tribe of black Africans and their European and
Middle Eastern cousins suggests that if there is such a thing as race,
it isn't a matter of skin color or a prominent nose.
Take
a look at the Irish. Using techniques similar to those that the British
geneticists had used in their search for Jewish continuity, molecular
biologists at Trinity College in Dublin combined research into ancient
Irish surnames with DNA analysis. They substantiated the claim that men
from Connaught, a western province, were descended from a population of
hunter-gatherers who migrated there 9,500 years ago from the Near East.
They, in turn, are thought to have descended from a group that had occupied
Europe an estimated 30,000 years ago, after the Neanderthals had left,
and settled in northern Spain before some of them continued on to Ireland.
The Irish may not look like their cousins the Basques, who stayed put
in the area of what is today the border between Spain and France, but
many of them carry the same telltale genetic marker.
The
six billion human beings alive on the Earth today have very different
phenotypes. That is, there are obvious differences in our skin color,
hair color and texture, facial shape, facial features, body size and proportions.
In the eighteenth century, Carolus Linnaeus, the Swedish scholar who created
the first scientific classification of animal species, was among the first
to attempt a scientific description of the subspecies, or "races," that
distinguish human beings. Many variations followed. Usually these efforts
identified three or four races, most commonly called Negroid or black,
Caucasian or white, Mongoloid or yellow, and Amerindian or red. By the
nineteenth century, the system builders linked these physical traits to
sexual practices and moral character or to academic skill. Not surprisingly,
these supposedly "scientific" racial attributes reflected the biases of
the European or American (certainly Caucasian) males who devised the system.
For example, British writers tended to label dark-skinned, narrow-featured
inhabitants of the Indian subcontinent as members of the Negroid race,
reflecting their colonial prejudices, whereas Americans, who had no imperial
axes to grind, tended to consider such people as Caucasian.
The
first challenge to the categorizing of human beings according to these
theories came from the anthropologist Franz Boaz. He argued that most
of the differences between people were cultural, not physical, and that
whatever physical differences did exist were too muddled to make sense.
Boaz's argument was substantiated by studies of human migrations, language
affinities and, after the 1940s, by the study of blood-group frequencies.
Blood
is a curious substance with an often-mystical role in human religious
practices. Flowing blood indicates life. The natural release of blood
in women of childbearing age, the ancient practice of purging blood from
the sick, as well as the ritualistic drinking of blood as a Christian
sacrament, place this particular bodily fluid in a special symbolic category.
We speak
of someone having "Italian blood" or "Chinese blood," of "bad blood" and
"good blood," but there is no such thing. With a few minor exceptions,
the four blood groups-A, B, AB and O-are found in all human populations.
The A blood of a Norwegian is compatible with the A blood of a Zimbabwean,
as the type O blood of a Vietnamese can be successfully transfused into
a Peruvian. There are, as in most things human, a few fascinating anomalies:
a large percentage of Germans have the same distribution of blood types
as do a large number of New Guineans, and similarly, a high percentage
of Estonians show nearly the same distribution as a high percentage of
Japanese. The distribution patterns of the human blood groups tell us
nothing about the alleged races of mankind.
DNA,
however, is altogether different. Genetic information, such as that linking
the dark-skinned Lemba to the beige-colored European Jews, effectively
challenges efforts to divide humankind into any racial groups at all.
Today most anthropologists, biologists and geneticists who use the word
"race" understand it as verbal shorthand to describe a few visible phenotypical
characteristics with no scientific meaning.
Skin
color, body shape and facial features turn out to be superficial characteristics
that seem to have arisen in response to local environmental conditions.
The differences between members of any one so-called race are usually
greater than the similarities that supposedly mark them off from members
of another "racial" group.
Take
skin color, the most obvious "racial" marker. Variations in skin color
are based on the amount of a chemical called melanin. Many scientists
believe that since melanin protects the skin from damage produced by exposure
to the ultraviolet rays of the sun, those people who live in areas where
they are likely to be exposed to a great deal of sunlight-close to the
equator or in open deserts-are likely to have adapted to their environment
by having more individuals with a lot of melanin survive to the age of
reproduction and therefore have darker skin than people who live in temperate
regions. Others believe that varieties of skin color have more to do with
sexual selection. They believe that in some communities females were attracted
to darker- or lighter-skinned males, and so chose them as mates. But however
the localized variations in skin color evolved, there are no rigidly definable
categories. People come in colors that range from the very darkest among
populations that are generally dark-skinned to the very lightest among
light-skinned people and cannot be divided into separate "races."
This
does not mean that we cannot speak of people as members of distinct ethnic
groups or diverse human populations. Individuals inherit their genes from
their parents, who inherited them from their parents, and so on back through
time. To the degree that our ancestors lived in one area of the world
for many generations and therefore chose their mates from within a finite
pool of people, some specifics of a genetic heritage will have emerged.
The genome of Australian aborigines, for example, will differ ever so
slightly from that of the Inuit people who have lived in the Arctic.
DNA
analysis has recently opened a door to new information about the very
origins of the human race. A team of scientists at Emory University School
of Medicine, using DNA analysis of the mitochondrial material carried
only in egg cells and therefore through the lines of female descent, and
a similar group working with DNA analysis of the Y-chromosome male line,
have both traced the genetic history of our species back to one common
ancestor of each sex who lived in central Africa approximately 150,000
years ago. Their work implies that everyone living today is descended
from these two people. Of course, this genetic Adam and Eve were not the
only humans alive in their day, but evidence suggests that all of the
descendants of their peers died out centuries, even millennia, ago.
The
same DNA patterns that point to our being just one big happy family also
reveal just when and how it was that some of our clan first moved away
from home. Tiny variations in DNA among people from different parts of
the world indicate that some folks left Africa and settled in Asia between
fifty-three thousand and seventy-three thousand years ago; others moved
toward Europe some forty thousand to fifty thousand years ago; and some
of the population that had settled in Asia and Europe moved on the Americas
seven thousand to thirty-five thousand years ago. The Asians traveled
across the Bering Sea; the route the Europeans took is unknown.
Within
the populations living on a specific continent, geneticists have identified
a number of subgroups, some twenty-eight in all, that enable them to trace
the moments of people as they spread out, colonizing different regions
and then settling down to form distinct communities. Scholars have suggested
that there are correlations between these subgroups and various language
groups. For example, a linguist at Stanford University speculates that
there is a parallel between three major subgroups of American Indians
as evidenced by differences in their mitochondrial DNA and by the three
main language groups of the Amerindian population.
These
kinds of genetic patterns are already making it possible for people whose
ancestral history is tantalizingly vague to fill in gaps in their family
tree. A British company has announced that it will analyze the DNA of
European customers who submit a sample of cells from the inside of their
mouths and tell them from which of seven European subgroups they are descended.
A recently established registry for African Americans offers to match
samples of their DNA to that of people from different areas of western
Africa in an effort to help them discover their likely ethnic roots. Similarly,
adoptees or orphans who know little about their biological roots might
someday be able to identify where their biological forebears most likely
came from by consulting a kind of DNA-specific map of the world that would
correlate genetic markers with geographical locations.
Since
all people on Earth are descended from the same ancestors, our genetic
variations can be looked at as a record of the paths followed by subsequent
generations. In addition to verifying the genetic histories of the Lemba
tribesmen and the villagers of Connaught, DNA evidence was recently brought
to bear on a question that had baffled students of Finnish culture for
years. The Finns speak a language that has few connections to the Indo-European
tongues spoken by their neighbors. The closest linguistic cousin of Finnish
is the Magyar language spoken by Hungarians, even though the similarities
are not all that close. Perhaps the Finns' language preserves a snapshot
of the original population of Finland, which we know was conquered centuries
ago by invaders from the steppes of central Asia. Most historians have
long assumed that the invaders wiped out the local population. But others
interpret the preservation of the ancient language as a sign that the
conquerors and conquered intermarried. DNA evidence recently was used
to settle the argument. The mitochondrial DNA in contemporary Finnish
women indicates the persistence of genes from the aboriginal population.
After the invaders won the war and killed off the men who opposed them,
they mated with the local women, who transmitted the invaders' language
and genes to the present-day Finnish population.
DNA
evidence can even be used to validate personal histories based on oral
traditions that heretofore have been disparaged. For nearly two hundred
years, the descendants of Sally Hemings, a black slave who belonged to
Thomas Jefferson, handed down family legends that Jefferson was the father
of Hemings' six children. In 2000, after years of denying that the story
had any merit, the Thomas Jefferson Memorial Foundation, which owns the
Jefferson homestead at Monticello and speaks for many of the third president's
living descendants, acknowledged the results of a 1998 test comparing
the DNA of several current-day descendants of Jefferson and Hemings. The
test results concluded that a Jefferson male had probably been the father
of Hemings' youngest son, Eston. There is no evidence placing the only
other likely candidates-the president's brother or his nephews-at Monticello
during the time Hemings would have conceived Eston. Therefore, the foundation
president announced, the test "suggests the strong likelihood" that Jefferson
fathered one, and possibly all, of Hemings' children.
DNA
evidence can be used to validate or disprove the claims of people with
aspirations to royalty. Posthumous tests made it clear that a woman who
had convinced millions that she was Anastasia, daughter of the last Romanov
rulers of Russia, was, in fact, a German born to an ordinary family with
no ties of any kind to the family of the tsars. Conversely, DNA analysis
confirmed the assertion by loyalists to the Bourbon kings of France that
a heart that had been preserved by happenstance was really that of the
martyred 10-year-old son of Louis XIV.
Fruitful
as these exercises may be for historians, keepers of the flame of royalty,
and individuals and their families, the more general application of DNA
analysis linked to population subgroups lies in the area of medical research.
Some localized gene pools contain a high frequency of otherwise rare characteristics
that have made them fascinating study areas for geneticists. A single
mutation in an individual's genes some generations back probably provided
some kind of adaptive advantage and therefore spread rapidly as more people
with this mutation survived into adulthood and transmitted the gene to
their children and grandchildren. A good example of this is the sickle-cell
variation in some blood cells that confers a protection against malaria
to people living in parts of sub-Saharan Africa, southeast Asia and the
Mediterranean basin where malaria is common. The variation spread through
local populations, and their descendants retain a disproportionate likelihood
of carrying that trait even though they no longer live in malarial areas.
A single gene for the sickle-cell trait still protects against malaria.
But should someone inherit the sickle cell from both parents, the result
is a condition known as sickle-cell anemia, which is painful and life-limiting.
Similarly, Tay-Sachs disease is caused by a genetic anomaly that is thought
to confer some protection against tuberculosis and is unusually prevalent
among people of eastern European descent, particularly Jews, who may have
lived in squalid conditions where tuberculosis thrived. A double dose
of the Tay-Sachs gene results in a condition that stops a child's development
around the age of two and is usually fatal before the child's fifth birthday.
Sometimes
a community's genetic history is well enough known that the source of
a distinguishing condition can be traced to a single individual. This
so-called founder's effect explains the high incidence of conditions like
porphyria (symptoms include extreme sensitivity to light) among white
South Africans and Huntington's disease among the inhabitants of several
isolated Venezuelan villages.
Disease
clusters fascinate students of genetic transmission in large part because
they can be traced to mutations in one gene. But most inherited tendencies-
from cancers to talents in academic achievement, athletics, art or music-result
from the interplay among many genes and the effect of the individual's
environment on those genes.
Today,
many anthropologists speak of clines, or gradations, to distinguish between
degrees of genetic closeness that include differences in skin color, propensity
toward diseases, and all the other factors-visible and hidden-that make
us what we are. Geneticists speak of lineages, or haplotypes, when they
describe the different subgroups that have descended from our common ancestors.
The old distinctions between what were once called races persist in everyday
speech, but they are becoming linguistically and ideologically obsolete
and as far removed from science as the once exalted study of alchemy.
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